
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves—the nerves that transmit information and signals from the brain and spinal cord to and from the rest of the body. Symptoms of CMT usually begin in the feet and legs, causing muscle weakness and atrophy, but they may eventually affect the hands and arms. While CMT is not life-threatening, it can cause difficulties with everyday activities and emotional distress. This article will explore whether CMT causes muscle spasms and detail other symptoms of the disease.
| Characteristics | Values |
|---|---|
| Common Name | Charcot-Marie-Tooth Disease |
| Abbreviation | CMT |
| Type of Disease | A group of inherited conditions that damage the peripheral nerves |
| Gene Involved | Mutations in genes on the X chromosome that make proteins in the myelin sheath |
| Symptoms | Smaller, weaker muscles, foot deformities, nerve issues, muscle contractions, difficulty walking, loss of sensation, difficulty swallowing or speaking, breathing problems, numbness or tingling, inability to feel heat or pain sensations, creeping sensations in legs, chronic pain, loss or decrease in senses like vision and hearing |
| Severity | Varies from person to person, but not life-threatening |
| Treatment | Physical therapy, assistive devices, surgery, occupational therapy |
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What You'll Learn
- Charcot-Marie-Tooth disease causes muscle contractions and weakness
- It affects nerves that control muscle movement
- The condition can cause foot drop, leading to frequent tripping
- CMT damages sensory nerve fibres, causing tingling and burning sensations
- It can cause muscle wasting and scoliosis in severe cases

Charcot-Marie-Tooth disease causes muscle contractions and weakness
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves, which are the nerves found outside the main central nervous system (brain and spinal cord). CMT is caused by an inherited fault in one of the many genes responsible for the development of the peripheral nerves. This fault causes the nerves to become damaged over time. The disease is named after the three healthcare providers who first described it in 1886.
CMT affects both motor and sensory nerves. Motor nerves carry signals from the brain to the muscles, telling them to move. Sensory nerves carry sensations such as heat, cold, and pain back to the brain. As a result, CMT can affect muscle control and movement and how your senses work. CMT can cause muscle contractions and weakness. The muscles that control the feet, lower legs, forearms, and hands are most affected. Usually, weakness begins in the feet and ankles, making it difficult to lift the foot at the ankle, so that the toes point downward during walking. This condition is known as foot drop and causes frequent tripping. As the disease progresses, contractures in the hand can lock the fingers in a flexed position.
The symptoms of CMT vary from person to person but usually start in the feet and legs. Over time, the disease may also affect the hands and arms. Symptoms usually first appear between the ages of 5 and 15, although they sometimes do not develop until middle age or later. CMT is a progressive condition, meaning the symptoms slowly get worse, making everyday tasks increasingly difficult. However, it is not a fatal disease, and most people with CMT have a normal lifespan.
There are six main types of CMT, all of which are caused by a genetic mutation inherited from one or both parents. The most common form of CMT is caused by mutations in genes on the X chromosome that make proteins in the myelin sheath. Boys typically have moderate to severe symptoms starting in late childhood, while girls may have milder symptoms or none. CMT can be diagnosed by a neurologist through a complete nervous system exam and a review of family history.
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It affects nerves that control muscle movement
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that affect the peripheral nerves—the nerves that transmit information and signals from the brain and spinal cord to the rest of the body, and vice versa. CMT is caused by a defective gene that results in abnormalities in the nerves supplying the feet, legs, hands, and arms. It affects both motor and sensory nerves. Motor nerves carry signals from the brain to the muscles, telling them to move. Sensory nerves carry sensations, such as heat, cold, and pain, back to the brain.
CMT usually affects the muscles that control the feet, lower legs, forearms, and hands. Weakness often begins in the feet and ankles, making it difficult to lift the foot at the ankle, leading to a condition called foot drop. This causes frequent tripping, and as the condition progresses, the person develops an abnormal gait. CMT can also cause muscle contractures, where muscles shorten and lose their normal range of movement. In some cases, surgery may be required to correct these contractures and problems such as flat feet.
As CMT progresses, contractures in the hands can cause the fingers to lock in a flexed position. In rare cases, severe proximal weakness can lead to scoliosis or kyphosis, a curvature of the spine. CMT can also affect the muscles required for breathing, which can be dangerous, especially at night, and may require a nighttime breathing assistive device.
The symptoms of CMT vary from person to person but usually start in the feet and legs before affecting the hands and arms. Symptoms typically appear in adolescence or early adulthood but can also develop in midlife. They include muscle weakness, foot deformities, and nerve issues, such as numbness or tingling, and a loss of sensation. CMT is not a fatal disease, and most people with the condition have a normal life expectancy. However, it can significantly impact a person's quality of life by making everyday activities challenging.
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The condition can cause foot drop, leading to frequent tripping
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves. The peripheral nerves are found outside the main central nervous system (the brain and spinal cord) and are responsible for controlling the muscles and relaying sensory information, such as touch, from the limbs to the brain. CMT is caused by an inherited fault in one of the many genes responsible for the development of these peripheral nerves.
CMT usually affects the muscles that control the feet, lower legs, forearms, and hands. Weakness often begins in the feet and ankles and can manifest as foot drop—a difficulty lifting the foot at the ankle, causing the toes to point downward during walking. Foot drop can lead to frequent tripping, and as the condition progresses, those affected may develop an abnormal gait as they attempt to compensate for their increasing weakness.
Foot abnormalities and difficulty walking are usually the most serious problems associated with CMT. The condition can cause muscle weakness, and in some cases, the muscles in the feet may not receive the brain's signal to contract, making it more likely for the affected person to trip and fall. CMT can also lead to a loss of sensation in the feet, which can result in unnoticed injuries or infections. For example, a blister on the toe may get infected without the person realising it.
The symptoms of CMT can vary significantly from person to person. They usually start in the feet and legs but may eventually affect the hands and arms. Symptoms typically appear in adolescence or early adulthood but can also develop in midlife. While CMT is not a fatal disease and does not affect life expectancy, it can make everyday activities challenging and significantly impact a person's quality of life.
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CMT damages sensory nerve fibres, causing tingling and burning sensations
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves—the nerves that transmit information and signals from the brain and spinal cord to and from the rest of the body, as well as sensory information such as touch, back to the spinal cord and brain. CMT is also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy (PMA).
The symptoms of CMT usually start in the feet and legs, but they may eventually affect the hands and arms. Symptoms typically appear in adolescence or early adulthood but may also develop in midlife. The symptoms of CMT vary from person to person, with some people experiencing more severe symptoms than others.
CMT is caused by an inherited fault in one of the many genes responsible for the development of the peripheral nerves. This fault means that the nerves become damaged over time. The neurons that reach down the spine to the legs and feet are the longest, and these longer neurons are most likely to show the early effects of CMT.
While CMT is not a fatal disease, it can make everyday activities very difficult. CMT is considered a peripheral neuropathy because it affects nerves outside of the brain and spinal cord.
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It can cause muscle wasting and scoliosis in severe cases
Charcot-Marie-Tooth disease (CMT) is a group of inherited disorders that cause nerve damage, specifically to the peripheral nerves—the nerves outside of the brain and spinal cord. This condition usually affects muscle control and how individuals feel their feet and hands. It results in smaller, weaker muscles and can cause muscle contractions, difficulty walking, and foot deformities.
As CMT progresses, severe cases can lead to muscle wasting and scoliosis. The disease causes a slow progression of weakness and wasting in the distal muscles, which are the muscles furthest from the centre of the body. This muscle weakness can lead to contractures (stiffened joints) that result in deformities of the feet and hands. Over time, the bones around the affected joints shift into abnormal positions, causing further complications.
In rare cases, severe proximal weakness can lead to scoliosis, a side-to-side curvature of the spine. Scoliosis is often accompanied by other issues with bones, joints, or muscles, such as an abnormal formation of the hip joint. These complications can significantly impact an individual's quality of life, making daily activities challenging.
It is important to note that the effects of CMT vary greatly from person to person, and not all cases will lead to muscle wasting or scoliosis. Early diagnosis and treatment are crucial to help manage symptoms and maintain an individual's quality of life. Physical therapy, orthopedic devices, and, in some cases, orthopedic surgery may be recommended to address these complications.
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Frequently asked questions
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves. It affects both motor and sensory nerves. Motor nerves carry signals from the brain to the muscles, while sensory nerves carry sensations like heat, cold, and pain back to the brain. CMT is caused by a gene problem inherited from one or both parents.
Symptoms of CMT usually start in the feet and legs and may later affect the hands and arms. The disease can cause muscle weakness and atrophy, leading to foot drop and high arches. People with CMT may experience tingling, burning sensations, and numbness in the hands and feet. It can also lead to contractures and bone deformities, making walking difficult.
While CMT primarily causes muscle weakness and atrophy, it can also lead to muscle contractures, where muscles shorten and lose their normal range of movement. This can result in deformities and affect a person's gait, leading to frequent tripping and falls. While CMT may not directly cause muscle spasms, the associated muscle issues and gait abnormalities can indirectly contribute to muscle spasms.











































